dbVar for Gene (Select 284865) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7148280	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 18,985,739-21,081,116 , GRCh37.p13 chr22: 18,973,252-21,435,405	SLC9A3P2, RNU6-225P, 99 more genes
nsv7148270	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,838-20,508,931 , GRCh38.p12 chr22: 18,483,514-20,345,217	DGCR2, MIR4761, 79 more genes
nsv7148246	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,838-21,416,074 , GRCh38.p12 chr22: 18,339,130-21,061,785	ZDHHC8, FAM230E, 121 more genes
nsv7148214	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 20,609,932-21,576,553 , GRCh38.p12 chr22: 18,339,630-21,222,264	IGLL4P, LOC107985584, 129 more genes
nsv7148166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,838-20,307,561 , GRCh38.p12 chr22: 18,906,325-20,320,038	MIR6816, PRODH, 61 more genes
nsv7137215	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,916,842-20,311,810 , GRCh38.p12 chr22: 18,929,329-20,324,287	TSSK1A, ESS2, 60 more genes
nsv7137150	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,888-21,481,925 , GRCh38.p12 chr22: 18,339,130-21,127,636	LOC107985584, LINC00896, 125 more genes
nsv7098862	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 18,206,749-21,234,326 , GRCh37.p13 chr22: 18,689,516-21,588,615	GP1BB, IGLL4P, 132 more genes
nsv7098756	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,886-21,386,103 , GRCh38.p12 chr22: 18,339,130-21,031,814	CCDC188, MED15, 118 more genes
nsv7093409	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,888-21,570,386 , GRCh38.p12 chr22: 18,339,130-21,216,097	FAM247A, P2RX6P, 129 more genes
nsv7093403	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 19,184,000-21,416,024 , GRCh38.p12 chr22: 18,339,130-21,061,735	LOC105372862, RPL7AP70, 121 more genes
nsv7093402	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,894,078-21,414,817 , GRCh38.p12 chr22: 18,339,130-21,060,528	LOC100420103, P2RX6P, 121 more genes
nsv7093382	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,834,445-21,414,817 , GRCh38.p12 chr22: 18,339,130-21,060,528	DGCR8, SEPTIN5, 121 more genes
nsv7075430	inversion	1	nstd229	human		GRCh38 chr22: 18,971,418-20,267,248 , GRCh37.p13 chr22: 18,958,931-20,254,771	LINC00896, LOC105372861, 57 more genes
nsv6638022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,916,843-21,075,592 , GRCh38.p12 chr22: 18,339,130-20,721,304	FAM230J, LOC107985588, 107 more genes
nsv6638009	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,648,867-21,465,659 , GRCh38.p12 chr22: 18,166,100-21,111,370	KLHL22, THAP7-AS1, 130 more genes
nsv6637960	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 19,046,677-21,465,662 , GRCh38.p12 chr22: 18,339,130-21,111,373	TSSK2, LOC112268297, 125 more genes
nsv6637871	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 19,647,905-21,153,690 , GRCh38.p12 chr22: 18,339,130-20,799,402	GGTLC5P, C22orf39, 108 more genes
nsv6637788	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,916,843-20,311,858 , GRCh38.p12 chr22: 18,929,330-20,324,335	LINC00895, C22orf39, 60 more genes
nsv6637775	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,916,843-21,798,907 , GRCh38.p12 chr22: 18,339,130-21,444,618	CRKL, E2F6P3, 139 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Study Type

Subject Phenotype Status

Additional filters

Links from Gene

Items: 1 to 20 of 692

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Number of Variants: 20

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